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- source_evidence_literature type ECO_0000212 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion evidence source_evidence_literature NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion SIO_000772 20125191 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion wasDerivedFrom befree-20150227 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_assertion wasGeneratedBy ECO_0000203 NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP762274.RAMqLJkZ65q5W_7X3Fe5nBtcr0VRbmtMsg1RtFvSPFHxI130_provenance.